EP0246612B1 - Schmierölzusammensetzung - Google Patents

Schmierölzusammensetzung Download PDF

Info

Publication number
EP0246612B1
EP0246612B1 EP87107270A EP87107270A EP0246612B1 EP 0246612 B1 EP0246612 B1 EP 0246612B1 EP 87107270 A EP87107270 A EP 87107270A EP 87107270 A EP87107270 A EP 87107270A EP 0246612 B1 EP0246612 B1 EP 0246612B1
Authority
EP
European Patent Office
Prior art keywords
oxide
lubricating oil
oil composition
weight
compound
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
EP87107270A
Other languages
English (en)
French (fr)
Other versions
EP0246612A2 (de
EP0246612A3 (en
Inventor
Shigeo Mori
Chuzo Isoda
Satoshi Teshima
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
DKS Co Ltd
Original Assignee
Dai Ichi Kogyo Seiyaku Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=14703047&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP0246612(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Dai Ichi Kogyo Seiyaku Co Ltd filed Critical Dai Ichi Kogyo Seiyaku Co Ltd
Publication of EP0246612A2 publication Critical patent/EP0246612A2/de
Publication of EP0246612A3 publication Critical patent/EP0246612A3/en
Application granted granted Critical
Publication of EP0246612B1 publication Critical patent/EP0246612B1/de
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M107/00Lubricating compositions characterised by the base-material being a macromolecular compound
    • C10M107/02Hydrocarbon polymers; Hydrocarbon polymers modified by oxidation
    • C10M107/18Hydrocarbon polymers modified by oxidation
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M111/00Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential
    • C10M111/04Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential at least one of them being a macromolecular organic compound
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G65/00Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/02Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
    • C08G65/26Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L71/00Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
    • C08L71/02Polyalkylene oxides
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M101/00Lubricating compositions characterised by the base-material being a mineral or fatty oil
    • C10M101/02Petroleum fractions
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M101/00Lubricating compositions characterised by the base-material being a mineral or fatty oil
    • C10M101/02Petroleum fractions
    • C10M101/025Petroleum fractions waxes
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M105/00Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
    • C10M105/56Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing nitrogen
    • C10M105/58Amines, e.g. polyalkylene polyamines, quaternary amines
    • C10M105/60Amines, e.g. polyalkylene polyamines, quaternary amines having amino groups bound to an acyclic or cycloaliphatic carbon atom
    • C10M105/62Amines, e.g. polyalkylene polyamines, quaternary amines having amino groups bound to an acyclic or cycloaliphatic carbon atom containing hydroxy groups
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M107/00Lubricating compositions characterised by the base-material being a macromolecular compound
    • C10M107/20Lubricating compositions characterised by the base-material being a macromolecular compound containing oxygen
    • C10M107/30Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M107/32Condensation polymers of aldehydes or ketones; Polyesters; Polyethers
    • C10M107/34Polyoxyalkylenes
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M111/00Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M145/00Lubricating compositions characterised by the additive being a macromolecular compound containing oxygen
    • C10M145/18Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M145/24Polyethers
    • C10M145/26Polyoxyalkylenes
    • C10M145/32Polyoxyalkylenes of alkylene oxides containing 4 or more carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M145/00Lubricating compositions characterised by the additive being a macromolecular compound containing oxygen
    • C10M145/18Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M145/24Polyethers
    • C10M145/26Polyoxyalkylenes
    • C10M145/34Polyoxyalkylenes of two or more specified different types
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M145/00Lubricating compositions characterised by the additive being a macromolecular compound containing oxygen
    • C10M145/18Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M145/24Polyethers
    • C10M145/26Polyoxyalkylenes
    • C10M145/36Polyoxyalkylenes etherified
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M145/00Lubricating compositions characterised by the additive being a macromolecular compound containing oxygen
    • C10M145/18Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M145/24Polyethers
    • C10M145/26Polyoxyalkylenes
    • C10M145/38Polyoxyalkylenes esterified
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M169/00Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
    • C10M169/04Mixtures of base-materials and additives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/102Aliphatic fractions
    • C10M2203/1025Aliphatic fractions used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/106Naphthenic fractions
    • C10M2203/1065Naphthenic fractions used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
    • C10M2209/105Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing three carbon atoms only
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
    • C10M2209/105Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing three carbon atoms only
    • C10M2209/1055Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing three carbon atoms only used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/04Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2215/042Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/04Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2215/042Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives thereof
    • C10M2215/0425Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives thereof used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2020/00Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
    • C10N2020/01Physico-chemical properties
    • C10N2020/04Molecular weight; Molecular weight distribution
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/06Oiliness; Film-strength; Anti-wear; Resistance to extreme pressure
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/10Inhibition of oxidation, e.g. anti-oxidants

Definitions

  • This invention relates to lubricating oil compositions containing a mineral base oil and an oil-soluble polyalkylene oxide compound.
  • Mineral oil lubricants such as paraffinic or naphthenic petroleum oils, have been used for most lubricating purposes. However, they have certain disadvantages such as relatively low viscosity indices over varying temperatures and high susceptibility to oxidation.
  • Synthetic lubricating oils such as those of polyalkylene oxide type have been used as substitutes for mineral oil lubricants in certain area because of their relatively high viscosity indices in comparison with mineral oil lubricants.
  • polymeric alkylene oxides containing long chain alkylene oxide moieties are substantially freely soluble in aliphatic hydrocarbon liquids and may be mixed with paraffinic or naphthenic lubricating oil bases to improve their properties such as viscosity indices, load-carrying capacities, anti-oxidative properties, wear resistances and the like.
  • a lubricating oil composition consisting essentially of a paraffinic or naphthenic or a mixture of both types of mineral oils, and 5 to 60% by weight of the composition of a polyalkylene oxide compound of the formula: wherein
  • polyalkylene oxide compounds of the above type are disclosed in, for example, U.S. Patent No. 4 302 349 to Kosswig et al.
  • this compounds are surface active agents suitable for reducing the interfacial surface tension of oily phases with respect to water.
  • the polyalkylene oxide compounds may be prepared by reacting a starting active hydrogen compound R(H)z in the presence of a basic or acidic catalyst first with a C 2 -C 4 alkylene oxide and then with a Ce-C 4 o alkylene oxide.
  • starting active hydrogen compounds include aliphatic monoalcohols such as methanol, ethanol, butanol, lauryl alcohol, oleyl alcohol and stearyl alcohol; glycols such as ethylene glycol, propylene glycol and butylene glycol; polyols such as glycerine, trimethylolpropane, sorbitol and sucrose; phenols such as phenol, bisphenol A and hydroquinone; amines such as ammonia, ethylenediamine, triethylenediamine, n-butylamine, laurylamine, aniline and toluidine; carboxylic acids such as acetic acid, maleic acid and oleic acid.
  • aliphatic monoalcohols such as methanol, ethanol, butanol, lauryl alcohol, oleyl alcohol and stearyl alcohol
  • glycols such as ethylene glycol, propylene glycol and butylene glycol
  • polyols such as glycerine,
  • C 3 -C 4 alkylene oxides examples include propylene oxide and butylene oxide. Mixtures of these alkylene oxides may also be used. Propylene oxide alone is preferable.
  • Usable basic or acidic catalyst include sodium hydroxide, potassium hydroxide, sodium acetate, sodium methoxide, boron tetrafluoride and phosphoric acid.
  • the proportions of C 3 -C 4 alkylene oxide and C 6 -C 4 o alkylene oxide relative to the active hydrogen compound are selected so that the resulting adduct has a molecular weight of 500-100,000 and the C 6 -C 40 alkylene oxide content of 15 to 60%, preferably 20 to 50% by weight of the entire molecule.
  • the reaction may be carried out at a temperature of 100 ° C to 150 ° C at a pressure below 0.59 MPa.
  • the resulting polyalkylene oxide adducts are substantially freely soluble in aliphatic hydrocarbon liquids such as paraffinic or naphthenic mineral oil bases.
  • aliphatic hydrocarbon liquids such as paraffinic or naphthenic mineral oil bases.
  • polyalkylene oxides which are soluble in both aliphatic and aromatic hydrocarbon liquids while those soluble only in aromatic hydrocarbons are known.
  • the polyalkylene oxide compounds used in the present invention may be intermixed with a paraffinic or naphthenic or a mixture of both types of mineral oils at any proportion.
  • the proportions of the polyalkylene oxide compounds ranging from 5 to 60%, preferably from 10 to 50% by weight of the composition have been found advantageous.
  • the polyalkylene compounds may improve properties of the base oils including viscosity indices, load-carrying capacities, anti-oxidative properties, wear resistances and the like while retaining inherent beneficial properties of the base oils.
  • the composition may contain conventional additives such as anti-oxidants, rust preventors and the like.
  • An autoclave having stirring means was charged with 6 parts of propylene glycol and 5 parts of potassium hydroxide and then purged with nitrogen gas. 924 parts of propylene oxide were introduced to the autoclave at a pressure of 0.40 MPa and reacted at 130°C. Thereafter, 284 parts of nonene oxide were reacted at 130 ° C. Total reaction time was 4 hours.
  • This polyalkylene oxide compound has a viscosity of 250 mPas at 25 ° C, a nonene oxide content of 22%, and a molecular weight of 1284, and is freely soluble in liquid paraffin.
  • the polyalkylene oxide compound prepared in Example 1 was incorporated to a paraffinic mineral oil (150 neutral), a naphthenic mineral oil (500 neutral) or a commercial motor oil (SAE 30) at a concentration shown in Table 2 below.
  • the resulting compositions and control oils free of the polyalkylene oxide compound were subjected to a load-carrying capacity test using Soda's four-balls tester at 220 rpm. The results are shown in Table 2.
  • the polyalkylene oxide compound improved various properties of the base oils significantly.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Emergency Medicine (AREA)
  • Lubricants (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Polyethers (AREA)

Claims (7)

1. Schmierölzusammensetzung, im wesentlichen bestehend aus einem Paraffin- oder Naphten-Mineralöl oder einem Gemisch von beiden Mineralöltypen und, bezogen auf das Gewicht der Zusammensetzung, aus 5 bis 60 Gew.-% einer Polyalkylenoxidverbindung der allgemeinen Formel:
Figure imgb0006
worin
R den Rest einer Verbindung darstellt, welche 1 bis 8 aktive Wasserstoffatome aufweist, wobei die aktiven Wasserstoffatome entfernt sind,
n für 3 bis 4 steht,
m für 6 bis 40 steht,
x und y eine ganze Zahl bedeuten, und
z für 1 bis 8 steht;
wobei die Polyalkylenoxidverbindung ein Molekulargewicht von 500 bis 100 000 und einen C6-C40-Al- kylenoxidgehalt von 15 bis 60 Gew.-%, bezogen auf das gesamte Molekül, aufweist.
2. Schmierölzusammensetzung nach Anspruch 1, worin die -(CnH2nO)x-Einheit Polyoxypropylen ist.
3. Schmierölzusammensetzung gemäß Anspruch 1, worin die -(CmH2mO)y-Einheit von Cyclohexenoxid, Nonenoxid oder einem C12 bis C4o-alpha-Olefinoxid abgeleitet ist.
4. Schmierölzusammensetzung nach Anspruch 1, worin der Cs-C4o-Alkylenoxidgehalt 20 bis 50 Gew.- %, bezogen auf die Polyalkylenoxidverbindung, beträgt.
5. Schmierölzusammensetzung nach Anspruch 1, worin die Verbindung mit 1 bis 8 aktiven Wasserstoffatomen ein aliphatischer Monoalkohol, ein Glykol, ein Polyol, ein Amin, ein Phenol oder eine Carbonsäure ist; worin die -(CnH2nO)x-Einheit Polyoxypropylen ist; worin die -CmH2mO-Einheit Cyclohexenoxid, Nonenoxid oder ein C12-C40-alpha-olefinoxid ist; und worin der C6-C40-Alkylenoxidgehalt 20 bis 50 Gew.-%, bezogen auf die Polyalkylenoxidverbindung beträgt.
6. Schmierölzusammensetzung nach Anspruch 1 oder 5, worin R ein von n-Butanol, Ethylenglykol, Propylenglycol, Glycerin, Nonylphenol oder Bisphenol A abgeleiteter Rest ist.
7. Schmierölzusammensetzung, im wesentlichen bestehend aus einem Paraffin- oder Naphten-Mineralöl oder einem Gemisch von beiden Mineralöltypen und, bezogen auf das Gewicht der Zusammensetzung, aus 5 bis 60 Gew.-% einer Polyalkylenoxidverbindung der allgemeinen Formel:
Figure imgb0007
worin
R den Rest eines aliphatischen Monoalkohols, eines Glykols, eines Polyols, eines Amines, eines Phenols oder einer Carbonsäure mit 1 bis 8 aktiven Wasserstoffatomen darstellt, wobei die aktiven Wasserstoffatome entfernt sind,
n für 3 bis 4 steht,
m für 6 bis 40 steht,
x und y eine ganze Zahl bedeuten, und
z für 1 bis 8 steht,
wobei die Polyalkylenoxidverbindung ein Molekulargewicht von 500 bis 100 000 und einen Cs-C4o-AI- kylenoxidgehalt von 20 bis 50 Gew.-%, bezogen auf das gesamte Molekül, aufweist.
EP87107270A 1986-05-20 1987-05-19 Schmierölzusammensetzung Expired - Lifetime EP0246612B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP117086/86 1986-05-20
JP61117086A JPH06104640B2 (ja) 1986-05-20 1986-05-20 本質的に非芳香族系炭化水素化合物と相溶するポリオキシアルキレン化合物の製造方法

Publications (3)

Publication Number Publication Date
EP0246612A2 EP0246612A2 (de) 1987-11-25
EP0246612A3 EP0246612A3 (en) 1988-02-03
EP0246612B1 true EP0246612B1 (de) 1990-12-05

Family

ID=14703047

Family Applications (1)

Application Number Title Priority Date Filing Date
EP87107270A Expired - Lifetime EP0246612B1 (de) 1986-05-20 1987-05-19 Schmierölzusammensetzung

Country Status (5)

Country Link
US (1) US4793939A (de)
EP (1) EP0246612B1 (de)
JP (1) JPH06104640B2 (de)
KR (1) KR900004532B1 (de)
DE (1) DE3766538D1 (de)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8586520B2 (en) 2011-06-30 2013-11-19 Exxonmobil Research And Engineering Company Method of improving pour point of lubricating compositions containing polyalkylene glycol mono ethers

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3718374A1 (de) * 1987-06-02 1988-12-15 Bayer Ag Polyether, verfahren zu ihrer herstellung und schmiermittel, die diese polyether enthalten
DE68912454T2 (de) * 1988-07-21 1994-05-11 Bp Chem Int Ltd Polyetherschmiermittel.
DE4001043A1 (de) * 1990-01-16 1991-07-18 Basf Ag Motorenoel mit einem gehalt an phenolalkoxylaten
US5198135A (en) * 1990-09-21 1993-03-30 The Lubrizol Corporation Antiemulsion/antifoam agent for use in oils
GB9119291D0 (en) * 1991-09-10 1991-10-23 Bp Chem Int Ltd Polyethers
GB9127370D0 (en) * 1991-12-24 1992-02-19 Bp Chem Int Ltd Lubricating oil composition
US5370812A (en) * 1993-06-28 1994-12-06 Union Carbide Chemicals & Plastics Technology Corporation Lubricant compositions for refrigerators comprising polyalkylene glycol and a hydrocarbon solvent
WO1996011244A1 (en) * 1994-10-07 1996-04-18 Mobil Oil Corporation Multiphase lubrication
US5602085A (en) * 1994-10-07 1997-02-11 Mobil Oil Corporation Multi-phase lubricant
IT1277376B1 (it) * 1995-07-28 1997-11-10 Euron Spa Copolimeri a blocchi loro preparazione e loro uso come lubrificanti
DE19739271A1 (de) * 1997-09-08 1999-03-11 Clariant Gmbh Additiv zur Verbesserung der Fließfähigkeit von Mineralölen und Mineralöldestillaten
AR019107A1 (es) * 1998-04-27 2001-12-26 Dow Global Technologies Inc Polioles de alto peso molecular, proceso para su preparacion y uso de los mismos.
US6872694B2 (en) * 2000-03-16 2005-03-29 Kao Corporation Rheology control agent
US6916766B2 (en) * 2002-02-05 2005-07-12 Exxonmobil Research And Engineering Company Circulating oil compositions
US7651559B2 (en) 2005-11-04 2010-01-26 Franklin Industrial Minerals Mineral composition
US7833339B2 (en) 2006-04-18 2010-11-16 Franklin Industrial Minerals Mineral filler composition
FR2901801B1 (fr) * 2006-06-06 2009-06-12 Ceca Sa Sa Produits bitumineux et emulsions aqueuses a base de produits bitumineux et leurs utilisations
CN102471720A (zh) * 2009-07-23 2012-05-23 陶氏环球技术有限责任公司 可用作i-iv类烃油用润滑剂添加剂的聚亚烷基二醇
WO2013003405A1 (en) 2011-06-30 2013-01-03 Exxonmobil Research And Engineering Company Lubricating compositions containing polyalkylene glycol mono ethers
EP2726584B1 (de) 2011-06-30 2016-04-20 ExxonMobil Research and Engineering Company Verfahren zur verbesserung des stockpunktes von schmiermittelzusammensetzungen mit polyalkylenglykolmonoethern
US20130023455A1 (en) 2011-06-30 2013-01-24 Exxonmobil Research And Engineering Company Lubricating Compositions Containing Polyetheramines
US8685905B2 (en) 2012-03-29 2014-04-01 American Chemical Technologies, Inc. Hydrocarbon-based lubricants with polyether
US9850447B2 (en) 2013-05-23 2017-12-26 Dow Global Technologies Llc Polyalkylene glycols useful as lubricant additives for hydrocarbon base oils
EP3099765B1 (de) * 2014-01-28 2021-08-25 Basf Se Verwendung von alkoxylierten polyethylenglykolen in schmierölzusammensetzungen
JP6628355B2 (ja) * 2015-09-16 2020-01-08 出光興産株式会社 ポリエーテル化合物、粘度指数向上剤、潤滑油組成物、及びこれらの製造方法
EP3371287B1 (de) 2015-11-06 2020-03-25 Shrieve Chemical Products, Inc. Mit öl mischbare polyalkylenglykole und verwendungen davon

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2522155A (en) * 1946-10-18 1950-09-12 Shell Dev Lubricating compositions
US2819278A (en) * 1956-05-09 1958-01-07 Petrolite Corp Reaction product of epoxidized glycerides and hydroxylated tertiary monoamines
US3839212A (en) * 1968-12-27 1974-10-01 Texaco Inc Solubilizing process
US3789003A (en) * 1971-08-25 1974-01-29 Texaco Inc Solubilizing process
US4245004A (en) * 1978-05-26 1981-01-13 Basf Wyandotte Corporation Ethoxylated polytetramethylene glycols as fiber lubricants
DE2925628A1 (de) * 1979-06-26 1981-01-22 Huels Chemische Werke Ag Zur erniedrigung der grenzflaechenspannung oeliger phasen gegen wasser geeignete verbindungen

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8586520B2 (en) 2011-06-30 2013-11-19 Exxonmobil Research And Engineering Company Method of improving pour point of lubricating compositions containing polyalkylene glycol mono ethers

Also Published As

Publication number Publication date
EP0246612A2 (de) 1987-11-25
JPH06104640B2 (ja) 1994-12-21
KR870011231A (ko) 1987-12-21
KR900004532B1 (ko) 1990-06-29
DE3766538D1 (de) 1991-01-17
EP0246612A3 (en) 1988-02-03
JPS62273930A (ja) 1987-11-28
US4793939A (en) 1988-12-27

Similar Documents

Publication Publication Date Title
EP0246612B1 (de) Schmierölzusammensetzung
EP0440248B1 (de) Benzinzusammensetzung
JPS61501156A (ja) 置換カルボン酸およびその誘導体の製造方法
CN102124090A (zh) 水溶性金属加工油剂及金属加工用冷却剂
JPH05271259A (ja) ポリエーテルリン酸エステル類
KR0143779B1 (ko) 옥시-알킬렌 하이드록시 연결그룹을 갖는 긴 사슬의 지방족 하이드로카빌 아민 첨가제
US5576275A (en) Oil soluble polyalkylene glycols
US6063145A (en) Fuel compositions containing etheramine alkoxylates
CA2034144C (en) Engine oil containing phenol alkoxylates
US4298488A (en) Hydraulic fluid composition containing glycol ethers and borate ester
US3839212A (en) Solubilizing process
JPH04112856A (ja) 燃料及び無灰分分散剤としてのポリエーテル置換マンニッヒ基剤
US4851142A (en) Fluid loss additive for well drilling fluids
US4738797A (en) Aminocarboxylic acid-terminated polyoxyalkylene containing extreme pressure functional compositions
US5892130A (en) Oxyalkylene-modified polyoxybutylene alcohols
JPH066713B2 (ja) 作動液
JPH0117519B2 (de)
JPH0227393B2 (ja) Mizukeijunkatsuyusoseibutsu
CA1168649A (en) Lubricating compositions
AU774548B2 (en) Polyalkene alcohol polyetheramines and use thereof in fuels and lubricants
US5057122A (en) Diisocyanate derivatives as lubricant and fuel additives and compositions containing same
JPH0225957B2 (de)
US4192759A (en) Automotive brake fluid compositions including semipolar borates and heteroborates
US5217635A (en) Diisocyanate derivatives as lubricant and fuel additives and compositions containing same
CA1341005C (en) Fuel compositions and lubricating oil compositions containing very long chain alkylphenyl poly(oxyalkylene) aminocarbamate

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): DE FR GB NL

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

RHK1 Main classification (correction)

Ipc: C10M145/34

AK Designated contracting states

Kind code of ref document: A3

Designated state(s): DE FR GB NL

17P Request for examination filed

Effective date: 19880324

17Q First examination report despatched

Effective date: 19890321

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): DE FR GB NL

REF Corresponds to:

Ref document number: 3766538

Country of ref document: DE

Date of ref document: 19910117

ET Fr: translation filed
PLBI Opposition filed

Free format text: ORIGINAL CODE: 0009260

26 Opposition filed

Opponent name: BASF AKTIENGESELLSCHAFT, LUDWIGSHAFEN

Effective date: 19910601

PLBI Opposition filed

Free format text: ORIGINAL CODE: 0009260

NLR1 Nl: opposition has been filed with the epo

Opponent name: BASF AG

26 Opposition filed

Opponent name: BP CHEMICALS LIMITED

Effective date: 19910830

Opponent name: BASF AKTIENGESELLSCHAFT, LUDWIGSHAFEN

Effective date: 19910601

NLR1 Nl: opposition has been filed with the epo

Opponent name: BP CHEMICALS LIMITED

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 19930507

Year of fee payment: 7

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 19930510

Year of fee payment: 7

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 19930531

Year of fee payment: 7

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 19930602

Year of fee payment: 7

RDAG Patent revoked

Free format text: ORIGINAL CODE: 0009271

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: PATENT REVOKED

27W Patent revoked

Effective date: 19931213

GBPR Gb: patent revoked under art. 102 of the ep convention designating the uk as contracting state

Free format text: 931213

NLR2 Nl: decision of opposition